Skip to main content

Principle of NMR Spectroscopy

NMR-Spectroscopy Principle 

NMR spectroscopy involves the absorption of electromagnetic radiation in the radiofrequency region and the principle of NMR spectroscopy revolves around the non- zero value of nuclear spin i.e. I

 

S. No.

Number of Protons

Number of Neutrons

Nuclear Spin (I)

examples

1

even

even

0

6C12, 8O16

2*

            odd

even

Half integer

(1/2, 3/2, 5/2)

1H1, 9F19, 15P31

3**

            even

odd

Half integer

(1/2, 3/2, 5/2)

6C13

4***

             odd

odd

Full integer

7N14

*This is possible when both atomic number and mass number are odd.

 ** This is possible when both atomic number is even and mass number is odd.

 *** This is possible when both atomic number is odd and mass number is even.

 

In the absence of an external magnetic field, these spins are randomly oriented. However, on application of external magnetic field, their spins align in different possible orientations by aligning themselves either in the direction of the external magnetic field or in the direction opposite to the external magnetic field.

            Number of possible orientations = 2I+1

For I= ½ the possible orientations = 2x ½ +1 = 2


These spins are now separated by a fixed energy difference between them which is denoted by ΔE and this difference varies directly with the external applied magnetic field i.e. B0.

                                                                     ΔE  B0      and  ΔE  γ and

where, ΔE = energy difference between different spin states
 B = external applied magnetic field
h =  Planck's constant
ν = Precessional Frequency

γ = Gyromagnetic Ratio = magnetic moment /angular momentum

   ΔE = hν this makes, ν = γB0/2π

the interaction of spinning nucleus (smaller magnet) with the applied magnetic field generates a precessional motion in the spinning nucleus having a precessional frequency, ν. When this precessional frequency matches with frequency of sources’s radiowaves, the transition occurs from lower energy sate to higher. That’s why the process is known as Nuclear Magnetic Resonance. This absorption is recorded in the form of an NMR spectrum which provides significant information.




Get best price for notebook at India Mart:

1. Notebook https://dir.indiamart.com/impcat/notebook.html?utm_source=Meenajakhar-zu9fq&utm_medium=affiliate&utm_campaign=affiliate_pbp_apr_24&utm_content=4&utm_term=stationery&officesupplies 2. School Notebook https://dir.indiamart.com/impcat/school-notebook.html?utm_source=Meenajakhar-zu9fq&utm_medium=affiliate&utm_campaign=affiliate_pbp_apr_24&utm_content=5&utm_term=stationery&officesupplies 3. Writing Notebook https://dir.indiamart.com/impcat/writing-notebook.html?utm_source=Meenajakhar-zu9fq&utm_medium=affiliate&utm_campaign=affiliate_pbp_apr_24&utm_content=6&utm_term=stationery&officesupplies

Comments

Popular posts from this blog

Atomic Absorption Spectrometry

  Atomic Absorption Spectrometry is an absorption spectroscopic technique in which radiation of a particular frequency from a source is absorbed by non-excited neutral gaseous atoms  generated in an atomizer in their ground state. The light is absorbed in the UV-visible region and makes transitions to higher electronic energy levels. The amount  of light absorbed is quantified and this amount of absorption helps in determining the analyte concentration. (It follows Beer's Law) The concentration is measured by drawing a calibration curve  after calibrating instrument with a  standard of known concentration. Factors affecting  the amount of light absorbed Length of path transversed Concentration of absorbing atoms in the vapour state. The diagrammatic representation of Atomic Absorption Spectrometer are shown in the below diagram:  Components Used in Atomic Absorbance Spectrometer: 1. Hollow Cathode Lamp: Acts as source of radiation  It is a sha...

Updated list of questions after deletion of some topics for organic spectroscopy -II

  Q 1: Explain the effect of conjugation, hydrogen bonding and steric factor on vibrational frequency? Q 2: Application of Far, Near and Mid-IR spectroscopy? Q 3: Application of NMR Spetcroscopy? Q 4: Applications of Mass Spectrometry or its advantages over other spectroscopic techniques? Q 5: Why Carbon NMR is less sensitive than proton NMR or disadvantages of Carbon NMR over proton NMR Q 6: Advantages of FT-NMR over CW-NMR or difference between FT-NMR and CW -NMR Q 7: Short Notes on Following: a.  McLafferty rearrangement b.  Magnetic Anisotropy (for alkenes, alkynes, aromatic compounds and aldehydes with diagrams) c.  Mechanism of spin-spin interaction or splitting of signals d.  Coupling constant and factors affecting it e.  Long range coupling f.  Simplification of complex spectra (High Field strength, Double irradiation or spin-spin decoupling, Use of Shift Reagents) g.  Nitrogen rule. h.  EI (Electron Impact Ionization) i.  CI (Ch...

Gross and Specific Selection rules for different molecular spectroscopies

Gross selection rule   tells whether a molecule will be active or inactive in a particular Spectroscopy.   Specific selection rule tells about the allowed changes in the magnitude of energy when it is active in a particular Spectroscopy.     Rotational or Microwave Spectroscopy Gross selection rule: permanent dipole moment  Specific selection rule: ∆J = +1 or -1 ( for rigid rotor) 2. Vibrational or IR Spectroscopy Gross selection rule: change in dipole moment during vibrations Specific selection rule: ∆v = +1 or -1 ( for harmonic oscillator) 3. Raman Spectroscopy Gross selection rule: change in polarizability  Specific selection rule:   ∆J = 0, +2 or -2   ∆v = +1 or -1  4. Electronic or UV-Visible Spectroscopy Gross selection rule: No stringent rule Specific selection rule: ∆s = 0  and ∆l = +1 or -1 5. Nuclear Magnetic  Resonance or Radio waves Spectroscopy Gross selection rule: nuclear spin should be no zero  Specific se...